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        <dc:date>2013-05-17T16:39:03+02:00</dc:date>
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        <title>3D object counter - [References/Citation] </title>
        <link>http://imagejdocu.tudor.lu/doku.php?id=plugin:analysis:3d_object_counter:start&amp;rev=1368801543&amp;do=diff</link>
        <description>This plugin allows counting objects in 3D, and getting some measurements about each object found.


Author

Fabrice P. Cordelières, Institut Curie, Orsay (France). Fabrice.Cordelieres at curie.u-psud.fr


Features

This plugin:

	*  counts the number of 3D objects in a stack.
	*  quantifies for each found object the following parameters:
		*  Integrated density;
		*  Mean of the gray values;
		*  Standard deviation of the gray values;
		*  Minimum gray value;
		*  Maximum gray value;
		*  Median…</description>
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        <dc:date>2013-05-17T13:54:12+02:00</dc:date>
        <dc:creator>aatorrano</dc:creator>
        <title>Particle in Cell-3D - [References] </title>
        <link>http://imagejdocu.tudor.lu/doku.php?id=macro:particle_in_cell-3d&amp;rev=1368791652&amp;do=diff</link>
        <description>Particle_in_Cell-3D is an ImageJ Macro designed to quantify the uptake of macro- and nanoparticles by cells.

Input


Routines 1, 2 and 3:

	*  Confocal fluorescence image stack of a single cell with stained plasma membrane
	*  Respective image stack of nanoparticles</description>
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        <dc:date>2013-05-16T08:41:20+02:00</dc:date>
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        <title>FAQ: Are there performance statistics to compare against my system?</title>
        <link>http://imagejdocu.tudor.lu/doku.php?id=faq:technical:are_there_performance_statistics_to_compare_against_my_system&amp;rev=1368686480&amp;do=diff</link>
        <description>What is ImageJ's typical performance on various system configurations, and how does my machine compare to them?

ImageJ has a Benchmark utility you can run to evaluate your system's performance.


	*  Start up a fresh ImageJ.
	*  Choose File &gt; New Text Window from the menu.
	*  Paste in the benchmark test macro (in the blue box below, thanks to Gabriel Landini for providing it).
	*  Choose Macros &gt; Run Macro from the menu to execute the benchmark.
	*  Compare your results against the table below…</description>
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        <dc:date>2013-05-03T13:13:33+02:00</dc:date>
        <dc:creator>gadeamm</dc:creator>
        <title>NEURONPERSISTENTJ - [Installation] </title>
        <link>http://imagejdocu.tudor.lu/doku.php?id=plugin:utilities:neuronpersistentj:start&amp;rev=1367579613&amp;do=diff</link>
        <description>Introduction

This free code is an ImageJ plugin that allows one to detect the neuronal structure from image.

This plugin, is a joint work between the team &quot;Structural Synaptic Plasticity&quot; of The Biomedical Research Centre of La Rioja (CIBIR) and &quot;Programming and Symbolic Computation Team” of University of La Rioja.</description>
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        <dc:date>2013-04-29T22:00:53+02:00</dc:date>
        <dc:creator>gilbertbigras</dc:creator>
        <title>COLOR DECONVOLUTION: OPTIMIZING HANDLING OF 3D UNITARY OPTICAL DENSITY VECTORS WITH POLAR COORDINATES</title>
        <link>http://imagejdocu.tudor.lu/doku.php?id=plugin:color:colour_deconvolution:optimizing_selection_of_unitary_optical_density_vectors:start&amp;rev=1367265653&amp;do=diff</link>
        <description>INTRODUCTION


This software was designed to ease the determination of unitary optical density vectors used in the color decovolution plugin written by Gabriel Landini &lt;http://www.dentistry.bham.ac.uk/landinig/software/software.html&gt; and based on the original publication by Ruifrok and Johnston:Quantification of histochemical staining by color deconvolution.
The major idea of this imageJ plugin relies on the fact that 3D optical density unitary vectors (which are the core of the colour deconvolu…</description>
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        <dc:date>2013-04-19T18:35:28+02:00</dc:date>
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        <title>MSCS (Micropatterned Single Cell Sorting) - [Changelog] </title>
        <link>http://imagejdocu.tudor.lu/doku.php?id=plugin:analysis:micropatterned_single_cell_sorting_mscs_:start&amp;rev=1366389328&amp;do=diff</link>
        <description>use this plugin to sort micropatterned single cell images from high-throughput experiments.

Jean-Philippe Grossier
jp.grossier at gmail dot com

 handle 96well format images
 process multiple experiments/plates
 can sort different micropatterns according to their size</description>
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        <dc:format>text/html</dc:format>
        <dc:date>2013-04-12T23:14:19+02:00</dc:date>
        <dc:creator>tferreira</dc:creator>
        <title>Sholl Analysis - Corrected mistake in S definiton</title>
        <link>http://imagejdocu.tudor.lu/doku.php?id=plugin:analysis:asa:start&amp;rev=1365801259&amp;do=diff</link>
        <description>For the Fiji plugin, visit the Fiji website. For analysis of traced arbors have a look at Simple Neurite Tracer.



Introduction

[Sholl mask]

This ImageJ plugin performs 2D and 3D Sholl analysis on grayscale images of single neurons. Sholl is a popular technique used by neuroanatomists to describe neuronal arbors. The major advantages of this plugin over other implementations are:</description>
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        <dc:format>text/html</dc:format>
        <dc:date>2013-04-12T12:21:12+02:00</dc:date>
        <dc:creator>nshimirimana</dc:creator>
        <title>Plugins - [Analysis] </title>
        <link>http://imagejdocu.tudor.lu/doku.php?id=plugin:start&amp;rev=1365762072&amp;do=diff</link>
        <description>Descriptions and downloads for ImageJ plugins stored here. There are many more plugins in the ImageJ website.

Acquisition

	*  ImageJVI

Aligning

	*  Align_4
	*  Align_RGB_planes
	*  Align_Slice
	*  bUnwarpJ: consistent and elastic registration
	*  Image Stabilizer</description>
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        <dc:date>2013-04-12T12:13:43+02:00</dc:date>
        <dc:creator>nshimirimana</dc:creator>
        <title>Radial thickness measure - created</title>
        <link>http://imagejdocu.tudor.lu/doku.php?id=plugin:analysis:radial_thickness_measure:start&amp;rev=1365761623&amp;do=diff</link>
        <description>Measure the radial distribution of the cross section thickness within the region of interest(circle or a circular sector)


Robert Nshimirimana


Line selection measurement


This program will measure the radial distribution of the cross section thickness within the region of interest(circle or a circular sector)defined by the radius and the angular range. The thickness is  calculated along the line of each step angle from the center of the region of interest. The required inputs are: radius and…</description>
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        <dc:format>text/html</dc:format>
        <dc:date>2013-04-10T18:06:26+02:00</dc:date>
        <dc:creator>rkd8</dc:creator>
        <title>Mitophagy - [Author] </title>
        <link>http://imagejdocu.tudor.lu/doku.php?id=macro:mitpophagy_mitochondrial_morphology_content_lc3_colocalization_macro&amp;rev=1365609986&amp;do=diff</link>
        <description>Mitophagy

Introduction

Microtubule associated protein light chain 3(LC3) is a ubiquitin-like protein that binds to autophagosomes (AVs). Cellular biologists transfect mammalian cells with GFP tagged LC3 to track and follow the fate of AVs in the cell and to measure autophagic flux. Also, GFP-LC3 puncta that colocalize with mitochondria is a way to measure the initiation of mitochondrial autophagy, the catabolic process by which mitochondria are targeted for lysosomal degradation.</description>
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        <dc:format>text/html</dc:format>
        <dc:date>2013-04-10T18:03:49+02:00</dc:date>
        <dc:creator>rkd8</dc:creator>
        <title>Mitochondrial Morphology - [Download] </title>
        <link>http://imagejdocu.tudor.lu/doku.php?id=plugin:morphology:mitochondrial_morphology_macro_plug-in:start&amp;rev=1365609829&amp;do=diff</link>
        <description>Mito-Morphology Macro

Introduction

This macro allows you to measure mitochondrial interconnectivity and elongation from epifluorescence micrographs of cells immunostained for mitochondria or transiently expressing mitochondrially targeted GFP. This macro was designed by Ruben K. Dagda while working at the Chu lab at the University of Pittsburgh (2010).
 This macro only works on the old version of Image J, and for versions 1.44 and 1.46.</description>
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        <dc:format>text/html</dc:format>
        <dc:date>2013-04-10T10:40:46+02:00</dc:date>
        <dc:creator>mutterer</dc:creator>
        <title>FigureJ - [Documentation] </title>
        <link>http://imagejdocu.tudor.lu/doku.php?id=plugin:utilities:figurej:start&amp;rev=1365583246&amp;do=diff</link>
        <description>This plugin achieves easy creation of image figures for publications, reports, projects.

Authors

Jerome Mutterer (CNRS) and Edda Zinck (HTW).

Contact: mutterer[at]ibmp.fr


Credits

	*   CNRS, IBMP, Strasbourg, France
	*   HTW, Berlin, Germany
	*   Carl Zeiss Microscopy supports this project as part of the Open Application Development initiative.</description>
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